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NCT06076564: LASSO

Leveraging Psychological Autopsies to Accelerate Research Into Stimulant Overdose Mortality

Completed Last updated 27 November 2024
What this trial tests

trial in Stimulant Overdose in 176 participants. Completed in 12 February 2024.

Timeline
6 June 2022
Primary endpoint
12 February 2024
12 February 2024

Quick facts

Lead sponsorSan Francisco Department of Public Health
StatusCompleted
Study typeOBSERVATIONAL
Enrollment176
Start date6 June 2022
Primary completion12 February 2024
Estimated completion12 February 2024
Sites1 location across United States

Conditions studied

Sponsor

San Francisco Department of Public Health

Who can join

18 and older, any sex, with Stimulant Overdose or Overdose Accidental. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In the LASSO study, the investigators will identify 100 stimulant overdose decedents (divided among stimulant-only, and stimulant with fentanyl), conduct informant interviews (including scales and qualitative data), and gather data from the postmortem investigation (e.g., vital records, toxicology, autopsy, case narrative, death scene photographs) and medical record abstraction. Subsequently, study staff will conduct qualitative interviews with 40-60 living people who use stimulants (aiming for half methamphetamine, half cocaine) to explore elements of resilience and risk reduction strategies. This study aims to contribute to the eventual design of interventions to reduce stimulant overdose mortality.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other San Francisco Department of Public Health trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing